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Hemoglobin
international journal for hemoglobin research
Volume 41, 2017 - Issue 4-6
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Short Communication

Hb F Levels in Indian Sickle Cell Patients and Association with the HBB Locus Variant rs10128556 (C>T), and the HBG XmnI (Arab-Indian) Variant

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Pages 317-320 | Received 13 Oct 2017, Accepted 22 Nov 2017, Published online: 09 Jan 2018

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Licínio Manco, Raquel Santos, Catarina Rocha, Luís Relvas, Celeste Bento, Tabita Maia, Verónica Gomes, António Amorim & Maria J. Prata. (2022) Hb F Levels in β-Thalassemia Carriers and Normal Individuals: Known and Unknown Quantitative Trait Loci in the β-Globin Gene Cluster. Hemoglobin 46:3, pages 168-175.
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Fatima-Zahra Alaoui-Ismaili, Achraf Laghmich, Naima Ghailani-Nourouti, Amina Barakat & Mohcine Bennani-Mechita. (2020) XmnI Polymorphism in Sickle Cell Disease in North Morocco. Hemoglobin 44:3, pages 190-194.
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Articles from other publishers (5)

Justin K. Kirkham, Jeremie H. Estepp, Mitch J. Weiss & Sara R. Rashkin. (2023) Genetic Variation and Sickle Cell Disease Severity. JAMA Network Open 6:10, pages e2337484.
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Fateen Ata, Zohaib Yousaf, Sundus Sardar, Saad Javed, Phool Iqbal, Ibraheem Khamees, Lujain Salahaldeen Malkawi & Mohamed A. Yassin. (2022) Protocol for “Genetic composition of sickle cell disease in the Arab population: A systematic review”. Health Science Reports 5:3.
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Shuang-Ping Ma, Hai-Rui Xi, Xu-Xia Gao, Jing-Min Yang, Ryo Kurita, Yukio Nakamura, Xian-Min Song, Hong-Yan Chen & Da-Ru Lu. (2021) Long noncoding RNA HBBP1 enhances γ-globin expression through the ETS transcription factor ELK1. Biochemical and Biophysical Research Communications 552, pages 157-163.
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Li Hu, Ling Huang, Yuanyuan Han, Tingting Jin, Juan Liu, Minmin Jiang, Xingmei Liu, Yuanyuan Li, Wenping Han, Bangquan An & Shengwen Huang. (2020) Association of polymorphisms in the HBG1‐HBD intergenic region with HbF levels . Journal of Clinical Laboratory Analysis 34:6.
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Françoise Bernaudin, Cécile Arnaud, Annie Kamdem, Isabelle HauFrançoise LelongRalph EpaudCorinne Pondarré & Serge Pissard. (2018) Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea. Blood Advances 2:6, pages 626-637.
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